A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590742



Internal ID20963813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:83952013..85834110hg38UCSC Ensembl
chr16:83985618..85867716hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg381882098
hg191882099
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240857
Samples
Known GenesADAD2, ATP2C2, C16orf74, COTL1, COX4I1, CRISPLD2, DNAAF1, EMC8, FAM92B, GINS2, GSE1, HSDL1, KCNG4, KIAA0513, KLHL36, LINC00311, LOC400548, MBTPS1, MIR1910, MIR5093, MIR7851, NECAB2, OSGIN1, SLC38A8, TAF1C, TLDC1, USP10, WFDC1, ZDHHC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590742
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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